About: Ludger A Wessjohann

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher ORCID ID = 0000-0003-2060-8235

Attributes	Values
rdf:type	Item
description	研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) জার্মান গবেষক (bn) chercheur allemand (fr) ikertzaile alemaniarra (eu) investigador alemany (ca) investigador alemán (es) investigador alemán (gl) investigador alemán (ast) investigador alemão (pt) ricercatore tedesco (it) researcher ORCID ID = 0000-0003-2060-8235 (en)
rdfs:label	Ludger A Wessjohann (ca) Ludger A Wessjohann (en) Ludger A Wessjohann (nl) Ludger A Wessjohann (sl) Ludger A Wessjohann (ast)
skos:prefLabel	Ludger A Wessjohann (ca) Ludger A Wessjohann (en) Ludger A Wessjohann (nl) Ludger A Wessjohann (sl) Ludger A Wessjohann (ast)
name	Ludger A Wessjohann (ca) Ludger A Wessjohann (en) Ludger A Wessjohann (nl) Ludger A Wessjohann (sl) Ludger A Wessjohann (ast)
given name	wds:Q60960357-9487205d-4013-4f59-aedd-e453e7835867
given name	Ludger
instance of	wds:Q60960357-9D2A405B-656A-4E83-A91D-0508ED1F49B3
instance of	Homo sapiens
Google Scholar author ID	wds:Q60960357-8d866095-4d3b-e948-b569-0e3b8fd4f663
Google Scholar author ID	Q7dxk3sAAAAJ
skos:altLabel	LA Wessjohann (en) Ludger Wessjohann (en)
occupation	wds:Q60960357-8d5279ef-4a66-d842-4f17-f30e6806c8bb
employer	wds:Q60960357-28D798D1-A388-431F-9DE9-7E1B96C409E6 wds:Q60960357-E5B74CB2-D09E-4878-B598-6B23B466CD98
NUKAT ID	wds:Q60960357-B401F7A8-CAFD-4043-AFC0-4257637549E0
languages spoken, written or signed	wds:Q60960357-9D02A86A-913C-4006-B993-8CC487D5A026
sex or gender	wds:Q60960357-6fcf9064-4f8d-ac9e-259b-325882acd47c
ISNI	wds:Q60960357-8CB2BB2F-94A9-471F-89F0-EF6CB5EE5C06
VIAF ID	wds:Q60960357-9E52087D-A42D-4FB8-9D30-D22B01DC85C0
GND ID	wds:Q60960357-587dbf2a-4964-0630-db05-48052f3788b1
country of citizenship	wds:Q60960357-8248b08f-4d79-96fd-7fe3-094ddef83b99
date of birth	wds:Q60960357-3d4abbc8-4d08-a93e-1069-3dbd56443a8f
VIAF ID	http://viaf.org/viaf/6670148037716988350000
GND ID	https://d-nb.info/gnd/1119834872
occupation	researcher
employer	Leibniz Institute of Plant Biochemistry Free University of Amsterdam
NUKAT ID	n2018080578
languages spoken, written or signed	German
sex or gender	male
ISNI	0000000391077427
VIAF ID	6670148037716988350000
GND ID	1119834872
country of citizenship	Germany
date of birth	1961-01-01 00:00:00Z (xsd:dateTime)
ORCID iD	wds:Q60960357-977F2396-26F0-4B11-A7F2-E7771B489102
ORCID iD	https://orcid.org/0000-0003-2060-8235
ORCID iD	0000-0003-2060-8235
is owl:sameAs of	Ludger A Wessjohann
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q60960357
is author of	Influence of Pickling Process on and Metabolome as Determined Mass Spectrometry-Based Metabolomics Developmental changes in leaf phenolics composition from three artichoke cvs. (Cynara scolymus) as determined via UHPLC-MS and chemometrics Metabolomics driven analysis of artichoke leaf and its commercial products via UHPLC-q-TOF-MS and chemometrics. A new cardenolide from the roots of Streptocaulon tomentosum Cation-π and π-π stacking interactions allow selective inhibition of butyrylcholinesterase by modified quinine and cinchonidine alkaloids. Cm-p5: an antifungal hydrophilic peptide derived from the coastal mollusk Cenchritis muricatus (Gastropoda: Littorinidae) Cytotoxic effect of commercial Humulus lupulus L. (hop) preparations - In comparison to its metabolomic fingerprint Multiple multicomponent macrocyclizations including bifunctional building blocks (MiBs) based on Staudinger and Passerini three-component reactions Brunneins A-C, beta-carboline alkaloids from Cortinarius brunneus What can a chemist learn from nature's macrocycles?--a brief, conceptual view. Macrocycles rapidly produced by multiple multicomponent reactions including bifunctional building blocks (MiBs). Highly substituted tetrahydropyrones from hetero-Diels-Alder reactions of 2-alkenals with stereochemical induction from chiral dienes Mutational studies confirm the catalytic triad in the human selenoenzyme thioredoxin reductase predicted by molecular modeling The bladder tumor suppressor protein TERE1 (UBIAD1) modulates cell cholesterol: implications for tumor progression The functional role of selenocysteine (Sec) in the catalysis mechanism of large thioredoxin reductases: proposition of a swapping catalytic triad including a Sec-His-Glu state Epothilone D affects cell cycle and microtubular pattern in plant cells Hydrogen peroxide - production, fate and role in redox signaling of tumor cells Selenium in chemistry and biochemistry in comparison to sulfur Homoisoflavonoids from Ophiopogon japonicus Ker-Gawler Natural products - modifying metabolite pathways in plants Rapid generation of macrocycles with natural-product-like side chains by multiple multicomponent macrocyclizations (MiBs). Profiling of Arabidopsis secondary metabolites by capillary liquid chromatography coupled to electrospray ionization quadrupole time-of-flight mass spectrometry Multiple multicomponent macrocyclizations (MiBs): a strategic development toward macrocycle diversity Supramolecular compounds from multiple ugi multicomponent macrocyclizations: peptoid-based cryptands, cages, and cryptophanes Diversity oriented one-pot synthesis of complex macrocycles: very large steroid-peptoid hybrids from multiple multicomponent reactions including bifunctional building blocks Volatiles profiling in medicinal licorice roots using steam distillation and solid-phase microextraction (SPME) coupled to chemometrics The UBIAD1 prenyltransferase links menaquinone-4 [corrected] synthesis to cholesterol metabolic enzymes Phytochemical Profiles and Antimicrobial Activities of Allium cepa Red cv. and A. sativum Subjected to Different Drying Methods: A Comparative MS-Based Metabolomics Natural Products from Microalgae with Potential against Alzheimer's Disease: Sulfolipids Are Potent Glutaminyl Cyclase Inhibitors

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